Variant report

Variant	rs10063190
Chromosome Location	chr5:91630972-91630973
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10041056	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10055515	0.92[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs10055632	0.92[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs10057380	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10065964	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10068186	0.85[AMR][1000 genomes]
rs10073874	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13354246	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72777068	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72777069	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72777081	0.96[AFR][1000 genomes];0.91[EUR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91628400-91632800	Weak transcription	NHDF-Ad	bronchial
2	chr5:91628600-91632400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr5:91628600-91633200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:91628600-91633400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:91629000-91632200	Weak transcription	Fetal Heart	heart
6	chr5:91629000-91632600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links